EP2928563B1 - Zusammensetzung mit einem silikonharz und silikongummi, körperpflegeprodukte damit - Google Patents

Zusammensetzung mit einem silikonharz und silikongummi, körperpflegeprodukte damit Download PDF

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Publication number
EP2928563B1
EP2928563B1 EP13812289.0A EP13812289A EP2928563B1 EP 2928563 B1 EP2928563 B1 EP 2928563B1 EP 13812289 A EP13812289 A EP 13812289A EP 2928563 B1 EP2928563 B1 EP 2928563B1
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Prior art keywords
silicone
gum
composition
resin
units
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EP13812289.0A
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English (en)
French (fr)
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EP2928563A1 (de
Inventor
Anne Dussaud
Bhavna Rana
Susan Sperring
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Momentive Performance Materials Inc
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Momentive Performance Materials Inc
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/06—Emulsions
    • A61K8/062—Oil-in-water emulsions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/892—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a hydroxy group, e.g. dimethiconol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00—Preparations for care of the skin
    • A61Q19/001—Preparations for care of the lips
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/26—Optical properties
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/30—Characterized by the absence of a particular group of ingredients
    • A61K2800/33—Free of surfactant
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59—Mixtures
    • A61K2800/594—Mixtures of polymers

Definitions

  • This invention generally relates to silicone compositions and personal care products containing same. More particularly, the invention relates to silicone compositions containing blends of silicone resin(s) and silicone gum(s) and to personal care products providing shine or gloss, e.g., hair conditioners, hair sprays, hair gels, hair creams, lip glosses, and the like, formulated with such compositions.
  • shine or gloss e.g., hair conditioners, hair sprays, hair gels, hair creams, lip glosses, and the like, formulated with such compositions.
  • linear silicones of high molecular weight have been known for a long time to provide hair conditioning and increase hair luster.
  • linear silicones have a tendency to flow and do not provide acceptably stable films on hair fibers.
  • MQ silicone resin and linear silicone blends form a structured network which is widely used in silicone pressure sensitive adhesives. Such blends are also commonly used for transfer resistance of pigmented formulations in cosmetics, e.g., lipsticks, foundations, and the like. However, in these applications, the blends of silicone resin and linear silicones are tacky and do not provide the clean, non-tacky and smooth finish that would be required of an acceptable hair care product.
  • composition which comprises:
  • compositions containing the composition of this invention provide high luster while leaving the hair with a smooth feel and with little if any fiber clumping.
  • MT silicone resin (a) of the composition herein contains one or more M units, represented by the formula R 1 3 SiO 1/3 , and T units represented by the formula R 3 SiO 3/2 wherein each R 1 and R 3 is independently a hydroxyl radical or monovalent hydrocarbon radical.
  • Suitable monovalent hydrocarbon radicals R 1 and R 3 include acyclic hydrocarbon radicals, alicyclic hydrocarbon radicals and aromatic hydrocarbon radicals.
  • Preferred monovalent hydrocarbon radicals are alkyl radicals, aryl radicals and aralkyl radicals.
  • acyclic hydrocarbon radical means a straight or branched chain hydrocarbon radical, preferably containing up 22 carbon atoms, which may be saturated or unsaturated and which may contain one or more hetero atoms, e.g., oxygen, nitrogen, etc., and/or one or more functional groups and/or atoms, e.g., hydroxyl, halo, especially chloro and fluoro, and the like, in substitution of a like number of hydrocarbyl hydrogen atoms.
  • Suitable monovalent acyclic hydrocarbon radicals include, for example, alkyl, alkenyl, alkynyl, hydroxyalkyl, cyanoalkyl, carboxyalkyl, alkyloxy, oxaalkyl, alkylcarbonyloxaalkylene, carboxamide and haloalkyl, such as, for example, methyl, ethyl, sec-butyl, tert-butyl, octyl, decyl, dodecyl, cetyl, stearyl, ethenyl, propenyl, butynyl, hydroxypropyl, cyanoethyl, butoxy, 23,8-trioxadecanyl, carboxymethyl, chloromethyl, trifluoromethyl, and 3,3,3-trifluoropropyl.
  • alicyclic hydrocarbon radical means a radical containing one or more saturated hydrocarbon rings, preferably containing from 4 to 12 carbon atoms per ring, which may optionally be substituted on one or more of the rings with one or more alkyl radicals, each preferably containing from 2 to 6 carbon atoms per alkyl radical, halo radicals or other functional groups and which, in the case of a monovalent alicyclic hydrocarbon radical containing two or more rings, may be fused rings.
  • Suitable monovalent alicyclic hydrocarbon radicals include, for example, cyclohexyl and cyclooctyl.
  • aromatic hydrocarbon radical means a hydrocarbon radical containing one or more aromatic rings per radical which may optionally, be substituted on the aromatic rings with one or more alkyl radicals, each preferably containing from 2 to 6 carbon atoms per alkyl radical, halo radicals or other functional groups and which, in the case of a monovalent aromatic hydrocarbon radical containing two or more rings, may be fused rings.
  • Suitable monovalent aromatic hydrocarbon radicals include, for example, phenyl, tolyl, 2,4,6-trimethylphenyl, 1,2-isopropylmethylphenyl, 1-pentalenyl, naphthyl, anthryl.
  • aralkyl means an aromatic derivative of an alkyl group, preferably a (C 2 -C 6 )alkyl group, wherein the alkyl portion of the aromatic derivative may optionally, be interrupted by an oxygen atom such as, for example, phenylethyl, phenylpropyl, 2-(1-naphthyl)ethyl, preferably phenylpropyl, phenyoxypropyl, biphenyloxypropyl, and the like.
  • silicone resin (a) contains 30 percent or greater, preferably 40 percent or greater, and more preferably 50 percent or greater, T units.
  • the ratio of M to T units ranges from 1:1 to 1:7 and the softening point of the resin ranges from 50° to 110°C.
  • Useful silicone resins of this type are disclosed in U.S. 2011/0040062 .
  • Silicone resin (a) has a number average molecular weight of 10,000 or greater, preferably up to 1,000,000, and more preferably from 10,000 to 500,000.
  • silicone gum (b) of the composition herein is selected from those silicones having a viscosity of from 0.3 - 200,000 and preferably from 750 - 2,000 Pa.s (from 300 to 200,000,000, and preferably from 750,000 to 2,000,000, centipoise (cps)) at 25°C.
  • the viscosity of silicone gum (b) can be readily measured employing known and conventional viscosity measurement apparatus and techniques.
  • silicone gum (b) exhibiting the foregoing viscosity characteristic contains M' units, represented by the formula R 1 3 SiO 1/2 , and one or more additional units selected from among D' units, represented by the formula R 5 2 SiO 2/2 , T' units, represented by the formula R 6 SiO 3/2 , and Q' units, represented by the formula SiO 4/2 , and mixtures thereof, wherein each R 4 , R 5 and R 6 is independently a hydroxyl radical or a monovalent hydrocarbon radical.
  • Suitable monovalent hydrocarbon radicals R 4 , R 5 and R 6 include acyclic hydrocarbon radicals, alicyclic hydrocarbon radicals and aromatic hydrocarbon radicals as defined and exemplified, supra.
  • Suitable silicone gums (b) are known and are commercially available.
  • the gums can be prepared according to the method disclosed in U.S. Patent No. 2,814,601 , wherein an appropriate siloxane is reacted with an aqueous acid in a closed system until the viscosity of the siloxane has become essentially constant. The product is then washed free of acid.
  • Specific examples of useful silicone gums (b), all from Momentive Performance Materials Inc. include Silsoft 1215 (dimethiconol gum in cyclodimethicone solvent D5, SE30 (dimethicone gum), Viscasil 60M (polydimethysiloxane gum) and Silsoft AX (alkyl-modified aminosilicone).
  • the invention provides for a non-crosslinked mixture of resin (a) and gum (b) that contains little or no crosslinkable functionality, e.g., R 1 and R 3 of resin (a) and R 4 , R 5 and R 6 of gum (b) will contain no more than a few crosslinkable groups, and/or crosslinking conditions will be avoided in the preparation of the mixtures of these silicones and their use in manufacturing the desired personal care product
  • the mixture of silicone resin (a) and silicone gum (b) herein must have a softening point of 50°C or greater, preferably 60°C or greater and more preferably 70°C or greater, and an elastic modulus at ambient temperature of 10 6 Pa or less, preferably 5x10 5 Pa or less and more preferably 3x10 5 Pa or less.
  • these characteristics of softening point and elastic modulus can be obtained with mixtures of silicone resin(s) (a) and silicone gum(s) (b) with weight ratios of resin(s) (a) to gum(s) (b) ranging from 0.4 to 6, preferably ranging from 0.5 to 5 and more preferably from 0.7 to 4.
  • the mixtures of silicone resin (a) and silicone gum (b) of this invention have softening points of 50°C or greater, which is to say, they are solids at ambient temperature, it may be advantageous for formulating a particular personal care product to dilute the mixture of silicone resin(s) (a) and silicone gum(s) (b) with one or more volatile organic solvents (c), e.g., an organosilicon-containing solvent such a ethyl trisiloxane, octyl trisiloxane, cyclodimethicone, and the like, and/or one or more other type organic solvents such as the volatile paraffinic solvents and the aromatic hydrocarbon solvents.
  • volatile organic solvents e.g., an organosilicon-containing solvent such a ethyl trisiloxane, octyl trisiloxane, cyclodimethicone, and the like, and/or one or more other type organic solvents such as the volatile paraffinic solvents
  • solvents examples include the C 5 -C 12 acyclic and cyclic alkanes, e.g., the straight chain and isomeric pentanes, hexanes, heptanes, octanes, nonanes, decanes, undecanes, dodecanes, etc., and their cyclic analogs, and aromatic solvents as, for example, exemplified by benzene, toulene, the xylenes, mesitylene, and the like.
  • C 5 -C 12 acyclic and cyclic alkanes e.g., the straight chain and isomeric pentanes, hexanes, heptanes, octanes, nonanes, decanes, undecanes, dodecanes, etc., and their cyclic analogs
  • aromatic solvents as, for example, exemplified by benzene, toulene, the xylenes, me
  • volatile organic solvents) (c) can generally be combined with mixtures of resin(s) (a) and gum(s) (b) in a weight ratio of solvent to resin/gum mixture from 200 to 0.1, preferably from 100 to 1 and more preferably from 60 to 5.
  • an organic solvent solution of resin (a) and gum (b) can be formulated as an aqueous or non-aqueous spray, an aqueous or non-aqueous foam or mousse, a water-in-oil (w/o) emulsion or oil-in-water (o/w) emulsion employing procedures well known in the art for providing hair care products.
  • the personal care formulations of the invention can also contain one or more other ingredients known for use in such products in known and conventional amounts such as humectants (panthenol, butylene glycol, sorbitol, glycerin, other polyols), amino acids, natural moisturizing factors (sodium PCA), nonionic waxes (fatty alcohols, ethoxylated waxes, glycerol stearate, bee waxes, paraffin waxes etc.), esters, triglyceride oils (olive oil, jojoba oil, sunflower oil, coconut oil, argan oil, grapeseed oil etc..), natural butters (shea butter, cocoa butter), emulsifiers (silicone emulsifiers, silicone polyether copolymers, organic emulsifiers), anionic or amphoteric surfactants (cocobetaine, SLES, isothionate, sugar surfactants), spreading agents such as silicone superspreaders, solid part
  • Silform Flex MT resin and SR1000 MQ resin are available from Momentive Performance Materials Inc.
  • Silsoft 1215 contains 15% by weight of dimethiconol gum in silicone solvent D5 and is available from Momentive Performance Materials Inc.
  • SE30 is a dimethicone gum also available from Momentive Performance Materials Inc.
  • Viscasil 60 M is a polydimethylsiloxane gum having a viscosity of about 60 Pa.s (60,000 cps) and is available from Momentive Performance Materials Inc.
  • Fiber clumping produced a significant volume reduction of the tress.
  • Volume reduction was measured by image analysis after the hair tress was stored 1 hour in a 90% RH humidity chamber. The tress volume was measured by counting the number of pixels of the tress area (A).
  • Hair coefficient of friction ⁇ was measured on a CSM tribometer (Needham, Ma), on a taut flat tress, with a flat stainless steel probe. Hair was considered smooth when ⁇ ⁇ 0.12.
  • Examples of mixtures of resin (a) and gum (b) blends and the results of treating hair with the mixtures are presented in Tables 1A and 1B below.
  • Examples A-F are comparative examples while examples 1 to 7 illustrate the claimed invention.
  • the mixtures of resin (a) and gum (b) were diluted in cyclodimethicone D5 to provide a 2% by weight solids solution.
  • a single bleached hair tress was immersed in each test solution for 1 min. Excess liquid was squeezed out and the tress was thoroughly dried to remove solvent D5 using a blow drier, the tress thereafter being placed in an oven at 45°C overnight By this procedure, approximately the same amount of silicone mixture was delivered to each hair tress sample.
  • Tress measurements were taken after equilibration in a 50% humidity chamber.
  • Example A is an untreated hair tress having low luster, low tack and a rough finish.
  • Example B the tress treated only with silicone gum had a very high luster but exhibited excessive clumping of its fibers resulting in the tress appearing greasy.
  • the mixtures of resin (a) and gum (b) of Examples C and D both of which had very low softening points, produced high tack films and excessive hair fiber clumping.
  • the mixtures of resin (a) and gum (b) of Examples E and F both of which had a high elastic modulus at room temperature, resulted in a hair with low luster and a rough finish.
  • the hair tresses of Examples 1-7 produced desirable properties of high gloss, low friction (smooth feel) and moderate volume reduction, i.e., no appreciable clumping. With a volume reduction between 40% and 60%, the hair tresses treated with the compositions of Examples 1-7 did not appear frizzy and the hair fibers avoided forming clumps as shown by the hair being able to flow freely.
  • the silicon mixtures of Examples 1-7 therefore fulfilled all major criteria for a well-formulated and functioning hair care product whereas Examples A-E failed to meet even one of these criteria.
  • Table 1A Mixtures of Resin (a) and Gum (b) Example % MQ % MT % T unit in Resin Gum (b) Weight Ratio of Resin (a) to Gum (b) Ex.
  • a Ex. B 0 0 Silsoft 1215 Ex. C 100 0 Silsoft 1215 0.5 Ex. D 100 0 Silsoft 1215 1.3 Ex. E 100 0 Silsoft 1215 3.1 Ex. F 100 0 Silsoft 1215 4.7 Ex. 1 100 85 Silsoft 1215 0.8 Ex. 2 100 85 Silsoft 1215 1.3 Ex. 3 100 85 Silsoft 1215 2.1 Ex. 4 100 85 Silsoft 1215 3.1 Ex. 5 100 85 Silsoft 1215 4.7 Ex. 6 20 80 68 Silsoft 1215 1.3 Ex.
  • the tress treated with a composition (Example 8) containing no cationic surfactant exhibited a high shine with no fiber clumping thus giving the hair a clean appearance with its fibers moving freely.
  • the hair treated with the composition containing cationic surfactant (Example G) appeared clumpy and greasy.
  • Table 3 sets forth the composition of O/W emulsions suitable for the formulation of hair care products.
  • Each of the illustrated compositions contains a mixture of silicone resin (a) and silicone gum (b) and no cationic surfactant.
  • Table 3: O/W emulsion examples Ingredient Tradename NCI* Description Example 9
  • Example 10 Example 11
  • Example 12 Example 13
  • Example 14 AMP-95 aminomethyl propanol 0.56 0.7
  • Aculyn 180 acrylates/hydroxyesters acrylates copolymer
  • Anionic polymer 2 Aculyn88 acrylates/steareth 20 methacrylate copolymer
  • Anionic polymer 5 Cellosize polymer peg-10 hydroxyethyl cellulose nonionic polymer Sepigel 305
  • Anionic polymer 5 Aristof lex AVC
  • Anionic polymer 2 Carbopol 980
  • Anionic polymer 0.9 Fixale G-100 AMP-acrylates/allyl meth acrylates copolymers
  • Table 4 below sets forth the composition of WO emulsions suitable for formation of hair care products.
  • the composition of example 17 does not fall within the scope of the invention as claimed.
  • Table 5 sets forth the formulation of a lip gloss product.
  • Table 5 Lip Gloss Formulation Ingredient Wt % MT resin 30 Viscasil 60M gum 15 Cyclodimethicone 54.8 Fragrance 0.2

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Claims (10)

  1. Zusammensetzung, welche umfasst:
    a) ein MT-Harz mit einer relativen Molekülmasse von über 10.000, das ein oder mehrere M-Einheiten der Formel R1 3SiO1/3 und T-Einheiten der Formel R3SiO3/2 enthält, wobei das Verhältnis von M- zu T-Einheiten von 1:1 bis 1:7 reicht und der Erweichungspunkt des MT-Harzes von 50° bis 110° C reicht, wobei jedes R1 und R3 unabhängig ein Hydroxylradikal oder ein monovalentes Kohlenwasserstoffradikal ist; und
    b) Silikonkautschuk,
    wobei die Mischung von MT-Harz (a) und Silikonkautschuk (b) nicht vernetzt ist und einen Erweichungspunkt von über 50°C und ein Elastizitätsmodul bei Umgebungstemperatur von weniger als 106Pa aufweist.
  2. Zusammensetzung nach Anspruch 1, wobei Silikonkautschuk (b) eine Viskosität von 0,3 bis 200.000 Pa·s (von 300 bis 200.000.000 Centipoise) bei 25°C aufweist.
  3. Zusammensetzung nach Anspruch 1, wobei Silikonkautschuk (b) ein oder mehrere M'-Einheiten der Formel R4 3SiO1/2 und ein oder mehrere zusätzliche Einheiten gewählt aus D'-Einheiten der Formel R5 2SiO2/2, T'-Einheiten der Formel R6SiO3/2 und Q'-Einheiten der Formel SiO4/2 und Mischungen derselben enthält, wobei jedes R4, R5 und R6 unabhängig ein Hydroxylradikal oder ein monovalentes Kohlenwasserstoffradikal ist.
  4. Zusammensetzung nach Anspruch 1, wobei Silikonkautschuk (b) mindestens eines von Dimethiconolkautschuk, Dimethiconkautschuk und Polydimethysilikonkautschuk ist.
  5. Zusammensetzung nach Anspruch 1, wobei das Gewichtsverhältnis von Silikonharz (a) zu Silikonkautschuk (b) von 0,4 bis 6 reicht.
  6. Zusammensetzung nach Anspruch 1, welche kationisch tensidfrei ist.
  7. Zusammensetzung nach Anspruch 1, welche weiterhin ein flüchtiges organisches Lösungsmittel für die Mischung aus Silikonharz (a) und Silikonkautschuk (b) umfasst.
  8. Körperpflegeprodukt, welches die Zusammensetzung nach einem der Ansprüche 1 bis 5 und
    a) flüchtiges organisches Lösungsmittel für die Mischung aus Silikonharz (a) und Silikonkautschuk (b) umfasst.
  9. Körperpflegeprodukt nach Anspruch 8, wobei das Körperpflegeprodukt ein kationisches tensidfreies Haarpflegeprodukt ist, in dem die Mischung aus Silikonharz (a) und Silikonkautschuk (b) in flüchtigem organischen Lösungsmittel aufgelöst ist.
  10. Zusammensetzung nach Anspruch 1, wobei das Körperpflegeprodukt ein Lipgloss ist.
EP13812289.0A 2012-12-04 2013-12-03 Zusammensetzung mit einem silikonharz und silikongummi, körperpflegeprodukte damit Active EP2928563B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13/693,474 US20140154199A1 (en) 2012-12-04 2012-12-04 Silicone-containing composition and personal care products containing same
PCT/US2013/072824 WO2014089044A1 (en) 2012-12-04 2013-12-03 Composition comprising a silicone resin and a silicone gum, personal care products containing the same

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EP2928563A1 EP2928563A1 (de) 2015-10-14
EP2928563B1 true EP2928563B1 (de) 2018-04-11

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US (2) US20140154199A1 (de)
EP (1) EP2928563B1 (de)
JP (1) JP6476128B2 (de)
CN (1) CN104822421B (de)
BR (1) BR112015013078B1 (de)
WO (1) WO2014089044A1 (de)

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US10369387B2 (en) 2017-02-28 2019-08-06 L'oreal Cosmetic compositions capable of forming a multilayer structure after application to a keratinous material
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US11712411B2 (en) 2016-03-31 2023-08-01 L'oreal Lip compositions capable of forming a multilayer structure after application to lips
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US10894010B2 (en) 2016-12-28 2021-01-19 L'oreal Cosmetic compositions which are homogenous in the bulk and capable of forming a multilayer structure after application to a keratinous material
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WO2014089044A1 (en) 2014-06-12
CN104822421A (zh) 2015-08-05
EP2928563A1 (de) 2015-10-14
CN104822421B (zh) 2018-09-11
JP2016503433A (ja) 2016-02-04
BR112015013078A2 (pt) 2017-07-11
JP6476128B2 (ja) 2019-02-27
US20140154199A1 (en) 2014-06-05
BR112015013078B1 (pt) 2020-10-27
US20160228349A1 (en) 2016-08-11

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